Canonical Allele Identifier: PA2826258178
Gene: SCN1A HGNC NCBI

Linked Data

ClinVar Variation Id: 2578400
ClinVar RCV Id: RCV003326176

Amino-acid Alleles

HGVS (amino-acid) Matching Registered Transcripts
NP_001189364.1:p.Leu209Pro
CA349074319
NM_001202435.3:c.626T>C